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Clinical risk factors for central lymph node metastasis in papillary thyroid carcinoma: a systematic review and meta‐analysis
Author(s) -
Qu Hui,
Sun Guorui,
Liu Yao,
He Qingsi
Publication year - 2015
Publication title -
clinical endocrinology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.055
H-Index - 147
eISSN - 1365-2265
pISSN - 0300-0664
DOI - 10.1111/cen.12583
Subject(s) - medicine , lymphovascular invasion , meta analysis , thyroid carcinoma , thyroid cancer , oncology , lymph node , retrospective cohort study , odds ratio , carcinoma , metastasis , thyroid , cancer
Summary Background Prophylactic central lymph node dissection ( CLND ) in clinically node‐negative patients remains controversial, and predictive factors for central lymph node metastasis ( CLNM ) in patients with papillary thyroid carcinoma ( PTC ) are not well defined. Herein, we conducted a systematic review to quantify the clinicopathologic factors predictive for CLNM in patients with PTC . Methods A systematic search of electronic databases (PubMed, Embase, Cochrane CENTRAL , Scopus and Wanfang Database) for studies published until July 2014 was performed. Cohort, case–control studies and randomized controlled trials that examined clinical risk factors of CLNM were included. Results Twenty‐five studies (4 prospective and 21 retrospective studies) involving 7,719 patients met final inclusion criteria. From the pooled analyses, male gender ( OR 1·93, 95% CI 1·40 to 2·64), tumour multifocality ( OR 1·93, 95% CI 1·62 to 2·30), tumour size >0·5 cm ( OR 3·48, 95% CI 2·24 to 5·41), capsular invasion ( OR 1·91, 95% CI 1·36 to 2·67), extrathyroidal extension ( OR 2·42, 95% CI 1·58 to 3·71), lymphovascular invasion ( OR 13·29, 95% CI 5·61 to 31·48) and lateral lymph node metastasis ( OR 14·33, 95% CI 5·34 to 38·50) were significantly associated with increased risk of CLNM , while age >45 years ( OR 0·65, 95% CI 0·51 to 0·83) and lymphocytic thyroiditis ( OR 0·70, 95% CI 0·53 to 0·92) resulted in decreased risk of CLNM . Bilaterality and tumour location were not significantly associated with CLNM development (all P > 0·05). Conclusions Our analysis identified several clinicopathologic factors associated with CLNM . These findings may guide the necessity and extent of prophylactic CLND and ultimately improve the outcomes of patients with PTC .